复发性透明细胞肉瘤及其对放化疗的反应

Anju Bansal, M. Kaur, G. Singh, R. Mohil
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引用次数: 0

摘要

透明细胞肉瘤是一种罕见的肿瘤,占所有软组织肿瘤的不到1%。它们是侵袭性病变,预后极差。这种肿瘤的临床诊断是具有挑战性的,需要组织病理学检查明确的特征。这种肿瘤的治疗方案尚不完善,大多数研究表明放化疗没有明确的作用。这是一个57岁男性的软组织透明细胞肉瘤病例,他表现为大腿上的固体囊性肿块,临床放射诊断为血肿。术后残余肿瘤通过放疗/化疗成功治疗,方式与黑色素瘤相似。因此,这篇文章也强调了放化疗在透明细胞肉瘤治疗中的作用,表明它可以像黑色素瘤一样更好地治疗,而不是像软组织肉瘤一样。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recurrent clear cell sarcoma and its responsiveness to chemoradiation
Clear cell sarcomas are rare tumours accounting for less than 1% of all soft tissue tumours. They are aggressive lesions with extremely poor prognosis. The clinical diagnosis of this tumour is challenging, requiring histopathologic examination for definite characterization. The treatment protocol for this tumour is not well-established, with most studies showing no clear cut role of chemoradiation. This is a case of clear cell sarcoma of soft tissue in a 57-year-old male who presented with a solid-cystic mass on the thigh and was diagnosed as hematoma clinicoradiologically. Post-operative residual tumour was treated successfully with radio/chemotherapy, in a manner similar to melanoma. This article, thus, also highlights the role of chemoradiation in the treatment of clear cell sarcoma, suggesting that it can be better treated like melanoma rather than like a soft tissue sarcoma.
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